1a8t: Difference between revisions

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New page: left|200px<br /><applet load="1a8t" size="450" color="white" frame="true" align="right" spinBox="true" caption="1a8t, resolution 2.55Å" /> '''METALLO-BETA-LACTAMA...
 
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[[Image:1a8t.gif|left|200px]]<br /><applet load="1a8t" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1a8t.gif|left|200px]]<br /><applet load="1a8t" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1a8t, resolution 2.55&Aring;" />
caption="1a8t, resolution 2.55&Aring;" />
'''METALLO-BETA-LACTAMASE IN COMPLEX WITH L-159,061'''<br />
'''METALLO-BETA-LACTAMASE IN COMPLEX WITH L-159,061'''<br />


==Overview==
==Overview==
BACKGROUND: High level resistance to carbapenem antibiotics in gram, negative bacteria such as Bacteroides fragilis is caused, in part, by, expression of a wide-spectrum metallo-beta-lactamase that hydrolyzes the, drug to an inactive form. Co-administration of metallo-beta-lactamase, inhibitors to resistant bacteria is expected to restore the antibacterial, activity of carbapenems. RESULTS: Biphenyl tetrazoles (BPTs) are a, structural class of potent competitive inhibitors of, metallo-beta-lactamase identified through screening and predicted using, molecular modeling of the enzyme structure. The X-ray crystal structure of, the enzyme bound to the BPT L-159,061 shows that the tetrazole moiety of, the inhibitor interacts directly with one of the two zinc atoms in the, active site, replacing a metal-bound water molecule. Inhibition of, metallo-beta-lactamase by BPTs in vitro correlates well with antibiotic, sensitization of resistant B. fragilis. CONCLUSIONS: BPT inhibitors can, sensitize a resistant B. fragilis clinical isolate expressing, metallo-beta-lactamase to the antibiotics imipenem or penicillin G but not, to rifampicin.
BACKGROUND: High level resistance to carbapenem antibiotics in gram negative bacteria such as Bacteroides fragilis is caused, in part, by expression of a wide-spectrum metallo-beta-lactamase that hydrolyzes the drug to an inactive form. Co-administration of metallo-beta-lactamase inhibitors to resistant bacteria is expected to restore the antibacterial activity of carbapenems. RESULTS: Biphenyl tetrazoles (BPTs) are a structural class of potent competitive inhibitors of metallo-beta-lactamase identified through screening and predicted using molecular modeling of the enzyme structure. The X-ray crystal structure of the enzyme bound to the BPT L-159,061 shows that the tetrazole moiety of the inhibitor interacts directly with one of the two zinc atoms in the active site, replacing a metal-bound water molecule. Inhibition of metallo-beta-lactamase by BPTs in vitro correlates well with antibiotic sensitization of resistant B. fragilis. CONCLUSIONS: BPT inhibitors can sensitize a resistant B. fragilis clinical isolate expressing metallo-beta-lactamase to the antibiotics imipenem or penicillin G but not to rifampicin.


==About this Structure==
==About this Structure==
1A8T is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacteroides_fragilis Bacteroides fragilis] with ZN and 061 as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Beta-lactamase Beta-lactamase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.2.6 3.5.2.6] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1A8T OCA].  
1A8T is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacteroides_fragilis Bacteroides fragilis] with <scene name='pdbligand=ZN:'>ZN</scene> and <scene name='pdbligand=061:'>061</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Beta-lactamase Beta-lactamase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.2.6 3.5.2.6] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A8T OCA].  


==Reference==
==Reference==
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[[Category: Beta-lactamase]]
[[Category: Beta-lactamase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Fitzgerald, P.M.D.]]
[[Category: Fitzgerald, P M.D.]]
[[Category: Grover, N.]]
[[Category: Grover, N.]]
[[Category: Toney, J.H.]]
[[Category: Toney, J H.]]
[[Category: Vanderwall, D.]]
[[Category: Vanderwall, D.]]
[[Category: 061]]
[[Category: 061]]
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[[Category: zinc]]
[[Category: zinc]]


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